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Formoterol

Catalog No.: GF11341Purity:>98.00%
Formoterol is a kind of long-acting β2-adrenergic receptor (β2AR) agonist.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


Formoterol
Cas No.: 73573-87-2
10mM (in 1mL DMSO)In Stock
$31.00
1
5mgIn Stock
$28.00
1
10mgIn Stock
$48.00
1
25mgIn Stock
$88.00
1
50mgIn Stock
$144.00
1
100mgIn Stock
$243.00
1
200mgIn Stock
$384.00
1

인용 문헌 (Citations)

1 publications이 제품을 사용한 연구자들의 논문

제품 설명 (Description)

Formoterol is a kind of long-acting β2-adrenergic receptor (β2AR) agonist [1]. Formoterol is widely used for symptomatic relief in asthma and control of chronic obstructive pulmonary disease (COPD) [2]. The therapeutic mechanism of Formoterol involves both bronchodilation through airway smooth muscle relaxation and anti-inflammatory activity [2].

Formoterol (0.1μM; 24h) inhibited secretion of TNFα in the bronchial epithelial (BE) cells infected with rhinovirus [3]. Formoterol (1μM; 24h) effectively reduced tert-butyl hydroperoxide-induced SH-SY5Y cell death [1]. Formoterol (0.1nM~1μM; 24h) inhibited the IgE-dependent release of histamine from human lung mast cells in a concentration-dependent manner [4].

Formoterol (1mg/kg; 4 weeks; s.c.) decreased the expression of Fbxo32 and Trim63 in muscle wasting Balb/c mice induced by doxorubicin hydrochloride [5]. Formoterol (1mg/kg; 2 weeks; i.p.) prevented abdominal aortic aneurysm formation in erythropoietin-induced ApoE−/− mice [2].

References:
[1] Chang J C, Chang H S, Chao Y C, et al. Formoterol acting via β2-adrenoreceptor restores mitochondrial dysfunction caused by parkinson's disease-related UQCRC1 mutation and improves mitochondrial homeostasis including dynamic and transport [J]. Biology, 2024, 13(4): 231.
[2] Zhang J, Cao Y, Ren R, et al. Medium-dose formoterol attenuated abdominal aortic aneurysm induced by EPO via β2AR/cAMP/SIRT1 pathway [J]. Advanced science, 2024, 11(15): e2306232.
[3] Bochkov Y A, Busse W W, Brockman-Schneider R A, et al. Budesonide and formoterol effects on rhinovirus replication and epithelial cell cytokine responses [J]. Respiratory research, 2013, 14(1): 98.
[4] Scola A M, Chong L K, Suvarna S K, et al. Desensitisation of mast cell beta2-adrenoceptor-mediated responses by salmeterol and formoterol [J]. British journal of pharmacology, 2004, 141(1): 163-171.
[5] De Lima Junior E A, Teixeira A A S, Silveira L S, et al. Formoterol reduces muscle wasting in mice undergoing doxorubicin chemotherapy [J]. Frontiers in oncology, 2023, 13: 1237709.

실험 프로토콜 (Protocol)

Cell experiment [1]:

Cell lines

Bronchial epithelial (BE) cells

Preparation Method

BE cells were obtained from airway brushings. Cells were incubated for 24h with Formoterol (0.01% DMSO drug vehicle), and then infected with 0.25 mL of rhinovirus-16 (5×106 plaque forming units [PFU]/mL). After 24h, cytokine secretion (TNFα) was analyzed.

Reaction Conditions

0.1μM; 24h

Applications

Formoterol inhibited secretion of TNFα in the cells.
Animal experiment [2]:

Animal models

Male Balb/c mice

Preparation Method

The mice received doxorubicin hydrochloride (DOX) to induce muscle wasting. One of the groups treated with Formoterol, and another not submitted to Formoterol treatment received saline solution (0.9%) by the corresponding route of administration. The mice were euthanized for sample collection after 4 weeks.

Dosage form

1mg/kg; 4 weeks; s.c.

Applications

Formoterol protected against DOX-induced increase in Fbxo32 and Trim63 gene expression.

References:
[1] Bochkov Y A, Busse W W, Brockman-Schneider R A, et al. Budesonide and formoterol effects on rhinovirus replication and epithelial cell cytokine responses [J]. Respiratory research, 2013, 14(1): 98.
[2] De Lima Junior E A, Teixeira A A S, Silveira L S, et al. Formoterol reduces muscle wasting in mice undergoing doxorubicin chemotherapy [J]. Frontiers in oncology, 2023, 13: 1237709.

제품 문서 (Product Documents)

Purity:>98.00%Appearance:A solid

화학적 특성 (Chemical Properties)

CAS 번호
73573-87-2
분자식
C19H24N2O4
분자량
344.4
용해도
DMSO : 250 mg/mL (725.90 mM; Need ultrasonic)
보관
-20°C
일반 주의사항
제품의 용해도 데이터에 따라 적절한 용매를 선택하십시오. 조제 후에는 반복적인 동결·해동을 피할 수 있도록 저장 용액을 소분하십시오.
저장 용액은 -80°C 보관 시 6개월 이내, -20°C 보관 시 1개월 이내에 사용하십시오.
용해도를 높이려면 튜브를 37°C로 데운 뒤 적절한 시간 동안 초음파 처리하십시오.
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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